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PubMed:10090885 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 0-39 DiseaseOrPhenotypicFeature denotes Autoimmune lymphoproliferative syndrome 0011158|0017979
T3 92-131 DiseaseOrPhenotypicFeature denotes Autoimmune lymphoproliferative syndrome 0011158|0017979
T5 133-137 DiseaseOrPhenotypicFeature denotes ALPS 0011158|0017979
T7 411-415 DiseaseOrPhenotypicFeature denotes ALPS 0011158|0017979
T9 967-971 DiseaseOrPhenotypicFeature denotes ALPS 0011158|0017979
T11 1188-1192 DiseaseOrPhenotypicFeature denotes ALPS 0011158|0017979
T13 1468-1472 DiseaseOrPhenotypicFeature denotes ALPS 0011158|0017979
T15 1535-1539 DiseaseOrPhenotypicFeature denotes ALPS 0011158|0017979
T17 1770-1774 DiseaseOrPhenotypicFeature denotes ALPS 0011158|0017979

NCBIDiseaseCorpus

Id Subject Object Predicate Lexical cue
T1 0-39 SpecificDisease:D056735 denotes Autoimmune lymphoproliferative syndrome
T2 92-131 SpecificDisease:D056735 denotes Autoimmune lymphoproliferative syndrome
T3 133-137 SpecificDisease:D056735 denotes ALPS
T4 144-206 CompositeMention:D008232|D007154 denotes disorder of lymphocyte homeostasis and immunological tolerance
T5 411-415 Modifier:D056735 denotes ALPS
T6 967-971 SpecificDisease:D056735 denotes ALPS
T7 1188-1192 Modifier:D056735 denotes ALPS
T8 1468-1472 Modifier:D056735 denotes ALPS
T9 1535-1539 Modifier:D056735 denotes ALPS
T10 1770-1774 SpecificDisease:D056735 denotes ALPS

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1709-1713 gene:6890 denotes APT1
T1 1770-1774 disease:C1328840 denotes ALPS
T2 1709-1713 gene:355 denotes APT1
T3 1770-1774 disease:C1328840 denotes ALPS
T4 1709-1713 gene:10434 denotes APT1
T5 1770-1774 disease:C1328840 denotes ALPS
R1 T0 T1 associated_with APT1,ALPS
R2 T2 T3 associated_with APT1,ALPS
R3 T4 T5 associated_with APT1,ALPS

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 92-102 HP_0002960 denotes Autoimmune
T2 144-166 HP_0004332 denotes disorder of lymphocyte